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FDA 510(k)

LOTUS Series 4 Enhanced Shears, LOTUS Series 5

N.º K: K221102 · 2022-12-15

SolicitanteSra Developments, Ltd.
Fecha de decisión2022-12-15
Código de productoLFL
DecisiónSubstantially Equivalent

Resumen del dispositivo

LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is the device name listed in this FDA 510(k) record. The listed applicant is Sra Developments, Ltd.. It received FDA 510(k) clearance on 2022-12-15 under 510(k) number K221102. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the LOTUS Series 4 Enhanced Shears, LOTUS Series 5?

LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is a medical device that received FDA 510(k) clearance on 2022-12-15. The listed applicant is Sra Developments, Ltd.. The 510(k) number is K221102.

When did LOTUS Series 4 Enhanced Shears, LOTUS Series 5 receive FDA 510(k) clearance?

LOTUS Series 4 Enhanced Shears, LOTUS Series 5 received FDA 510(k) clearance on 2022-12-15, under 510(k) number K221102.

Who is the listed applicant for LOTUS Series 4 Enhanced Shears, LOTUS Series 5?

The FDA 510(k) record lists Sra Developments, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOTUS Series 4 Enhanced Shears, LOTUS Series 5?

The FDA product code for LOTUS Series 4 Enhanced Shears, LOTUS Series 5 is LFL.

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Dispositivos relacionados (Código: LFL)

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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